- Short report
- Open Access
Photochemically induced ischemic stroke in rats
Experimental & Translational Stroke Medicine volume 4, Article number: 13 (2012)
Photothrombosis was introduced as a model of ischemic stroke by Watson et al. in 1985. In the present paper, we describe a protocol to induce photothrombotic infarcts in rats.
The photosensitive dye Bengal Rose is intravenously administered and a laser beam is stereotactically positioned onto the skull. Illumination through the intact skull leads to local activation of Bengal Rose, which results in free radical formation, disturbance of endothelial function and thrombus formation in illuminated small cortical vessels.
Photochemically induced infarcts cause long-term sensorimotor deficits, allow long-term survival and are particularly suitable to assess the effectiveness of neuroregenerative therapies in chronic stroke studies.
Stroke is the second most frequent cause of death and a leading cause of disability and cognitive impairment in developed countries [1, 2]. Ischemic stroke, which accounts for approximately 80% of strokes, constitutes a huge socioeconomic burden. Experimental models of cerebral ischemia have been developed to mimic human stroke, gain a better understanding of underlying pathophysiological mechanisms and foster the development of new therapies. Common models of focal and multifocal cerebral ischemia include the intraluminal thread middle cerebral artery occlusion (MCAo) model, surgical MCAo models using ligation, clipping, electrocauterization etc., endothelin-1-induced MCAo, and embolization models using blood clots or other embolus material for vessel occlusion (for review see ).
In 1985, Watson et al. introduced photothrombosis as a technique to induce focal cerebral infarction in the cortical vasculature of rats . The key mechanism is a photochemical reaction triggered by systemic administration of Bengal Rose and focal illumination of the skull. Illumination leads to local activation of Bengal Rose, which results in free radical formation, disturbance of endothelial function and local thrombosis in small cortical vessels [3, 5]. As compared to other animal models of stroke, animal preparation is simple because it does not require mechanical manipulation of cerebral blood vessels or parenchyma. Lesion size and location can be modulated by altering the irradiating intensity, duration of light exposure, beam position, and dye concentration. Apart from that, photothrombotic infarcts do not impede long-term survival and are thus suitable for chronic stroke studies [4, 6].
Materials and methods
Adult male Wistar rats (250 g)
S-ketamine hydrochloride 25 mg/ml (CEVA, Düsseldorf, D)
2% Xylazine (CEVA, Düsseldorf, D)
Bengal Rose (Sigma Aldrich, Steinheim, D)
4% paraformaldehyde (Merck KGaA, Darmstadt, D)
Stereotactic device (TSE Systems, Bad Homburg, D)
Laser EAGLE 60 series (G Laser Technologies, Kleinostheim, D)
Polyethylene catheter 30 m, 0,58 mm inner diameter (Smith Medical, Grasbrunn, D)
Heating device TKM-0902 (FMI, Backnang, D)
Surgical instruments: Scissors, Forceps, Razor, Stitching Set (Bayha, Tuttlingen, D)
All animal experiments must comply with national and institutional animal welfare regulations and require approval of an appropriate ethics committee. Our experimental protocols were appoved by our local ethics committee.
The rats are anesthetized with an intraperitoneal injection of ketamine hydrochloride (100 mg/kg body weight; Ketanest) and xylazine hydrochloride (8 mg/kg body weight). The depth of anesthesia is verified by foot pinches. If the rats are adequately anesthetized, there is no response of extremity (flexion or withdrawal).
The body temperature is monitored and maintained at 37°C by a thermostatically controlled heating pad.
The left femoral vein is exposed and cannulated with a polyethylene catheter for Bengal Rose infusion. The catheter is fixed with threads (Figure 1).
The rats are placed in a stereotactic frame (Figure 2).
The scalp is longitudinally incised (2.0-2.5 cm) and retracted to expose the skull. To avoid wound complications the skull exposure should be achieved with a single cut.
The periost is gently removed and coronal and sagittal sutures are identified (Figure 3).
A laser beam of 8 mm diameter (G Laser Technologies) and 560 nm wavelength is stereotactically positioned onto the skull 0.5 mm anterior to the bregma and 3.5 mm lateral from the midline (Figure 4).
The skull is illuminated for 20 minutes. During the first 2 minutes of illumination, Bengal Rose (0.133 mL/kg body weight, 10 mg/mL saline) is slowly injected through the previously inserted catheter.
Afterwards, the catheter is withdrawn and the skin is sutured.
After the surgical procedures, the rats are returned to their cages in a temperature-controlled room with 12-h light and dark cycles and food and water ad libitum.
Sham-operated animals receive the same treatment including Bengal Rose injection, but without illumination of the skull.
Step 1: 8 - 12 min.
Step 2: 1 min.
Step 3: 8 - 12 min.
Step 4: 2 - 4 min.
Step 5: 1 - 2 min.
Step 6: 1 - 2 min.
Step 7: 1 min.
Step 8: 20 min.
Step 9: 8 - 12 min.
The major outcome measures in preclinical stroke studies are infarct size and neurological deficits. Infarct volumes are determined either histologically from stained brain sections or non-invasively with MRI scans. In photochemically induced stroke, which is characterized by a rapidly evolving ischemic damage without salvageable penumbra, the infarct size is relatively stable and hardly responsive to neuroprotective therapies . Figures 5 and 6 illustrate size and location of photochemically induced infarcts. The severity of sensorimotor deficits can be assessed by a battery of behavioural tests, e.g. the cylinder test, the adhesive tape removal test, the forelimb placing test, the beam balance test, etc. (for review see ). Photothrombotic infarcts cause mild to moderate, long-term sensorimotor deficits, particularly well displayed by the cylinder test and the adhesive tape removal test [9, 10]. In our model, sensorimotor deficits are evident for at least four weeks [9, 10]. In addition, neurological scoring systems have been established to provide an overall assessment of the animal´s condition. However, the most commonly used neurological scoring systems are not sensitive enough to reliably reflect sensorimotor deficits subsequent to photochemically induced stroke. The Morris water maze is applied to assess cognitive deficits . Multiple histological analyses can be performed in order to elucidate molecular and cellular changes, including immunohistochemical stainings to analyze neurogenesis, dendritic and axonal plasticity, the postischemic inflammatory reaction, the upregulation of neurotransmitters, etc.
Animal preparation is simple and requires neither craniotomy nor mechanical manipulation of cerebral blood vessels or parenchyma .
Lesion size and location can be modulated by altering the irradiating intensity, duration of light exposure, beam position, and dye concentration .
Lesion size and location are highly reproducible [5, 6].
The procedure-associated mortality rate is low (< 10%).
Animals exhibit long-term sensorimotor deficits [9, 10].
Photothrombotic infarcts allow long-term survival .
Photothrombotic infarcts severely affect vessel walls and cause an early vasogenic edema atypical of human stroke .
The penumbra is missing in this model .
Due to the cortical location and the relatively small lesion size, sensorimotor deficits are minor in comparison to other stroke models .
Photothrombotic infarcts cause long-term sensorimotor deficits and allow long-term survival in chronic stroke studies. The infarct size is hardly responsive to neuroprotective therapies. However, the lack of responsiveness to neuroprotection in the acute phase allows a differentiation between neuroprotective and neuroregenerative effects, and, as a consequence, neuroregenerative therapies can be evaluated more precisely. Altogether, photochemically induced infarcts are particularly suitable to analyse the effectiveness of neuroregenerative therapies.
JM and MS shared senior authorship.
Donnan GA, Fisher M, Macleod M, Davis SM: Stroke. Lancet 2008, 371: 1612–1623. 10.1016/S0140-6736(08)60694-7
Lopez AD, Mathers CD, Ezzati M, Jamison DT, Murray CJ: Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data. Lancet 2006, 367: 1747–1757. 10.1016/S0140-6736(06)68770-9
Braeuninger S, Kleinschnitz C: Rodent models of focal cerebral ischemia: procedural pitfalls and translational problems. Exp Transl Stroke Med 2009, 1: 8. 10.1186/2040-7378-1-8
Watson BD, Dietrich WD, Busto R, Wachtel MS, Ginsberg MD: Induction of reproducible brain infarction by photochemically initiated thrombosis. Ann Neurol 1985, 17: 497–504. 10.1002/ana.410170513
Schroeter M, Jander S, Stoll G: Non-invasive induction of focal cerebral ischemia in mice by photothrombosis of cortical microvessels: characterization of inflammatory responses. J Neurosci Methods 2002, 117: 43–49. 10.1016/S0165-0270(02)00072-9
Macrae IM: Preclinical stroke research–advantages and disadvantages of the most common rodent models of focal ischaemia. Br J Pharmacol 2011, 164: 1062–1078. 10.1111/j.1476-5381.2011.01398.x
Diederich K, Quennet V, Bauer H, Muller HD, Wersching H, Schabitz WR, Minnerup J, Sommer C: Successful Regeneration After Experimental Stroke by Granulocyte-Colony Stimulating Factor Is Not Further Enhanced by Constraint-Induced Movement Therapy Either in Concurrent or in Sequential Combination Therapy. Stroke 2012, 43: 185–192. 10.1161/STROKEAHA.111.622159
Schallert T: Behavioral tests for preclinical intervention assessment. NeuroRx 2006, 3: 497–504. 10.1016/j.nurx.2006.08.001
Minnerup J, Kim JB, Schmidt A, Diederich K, Bauer H, Schilling M, Strecker JK, Ringelstein EB, Sommer C, Scholer HR, Schabitz WR: Effects of neural progenitor cells on sensorimotor recovery and endogenous repair mechanisms after photothrombotic stroke. Stroke 2011, 42: 1757–1763. 10.1161/STROKEAHA.110.599282
Minnerup J, Seeger FH, Kuhnert K, Diederich K, Schilling M, Dimmeler S, Schabitz WR: Intracarotid administration of human bone marrow mononuclear cells in rat photothrombotic ischemia. Exp Transl Stroke Med 2010, 2: 3. 10.1186/2040-7378-2-3
Morris R: Developments of a water-maze procedure for studying spatial learning in the rat. J Neurosci Methods 1984, 11: 47–60. 10.1016/0165-0270(84)90007-4
This study was supported from grants by the German Research Foundation (Deutsche Forschungsgesellschaft [DFG]; MI 1547/2-1).
The authors declare that they have no competing interests.
AS and MH carried out the experiments. AS drafted the manuscript. JM and MS supervised the experiments and helped drafting the manuscript. MH, JKS, KD and WRS contributed to conception and design and revised the manuscript. All authors read and approved the final manuscript.
Matthias Schilling and Jens Minnerup contributed equally to this work.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
Rights and permissions
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
About this article
Cite this article
Schmidt, A., Hoppen, M., Strecker, JK. et al. Photochemically induced ischemic stroke in rats. Exp & Trans Stroke Med 4, 13 (2012). https://doi.org/10.1186/2040-7378-4-13
- Experimental stroke
- Animal model